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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to October 2026.

37,269

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,085 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 2026

Most affected stateHawaii 200 recalls mention this state

State: GU ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 17, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: January 31, 2025Historical recordClass II

Sri Lakshmi Narasimhar Overseas

Product: Bliss Tree Millet Butter Ribbon Pakoda 200g UPC:890608745162…
Reason: Undeclared milk
Published: September 25, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 31, 2025Historical recordClass I

Sri Lakshmi Narasimhar Overseas

Product: Bliss Tree Millet Butter Murukku 200g UPC:8906087451631. Pac…
Reason: Undeclared sesame and milk
Published: September 25, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 31, 2025Historical recordClass II

Sri Lakshmi Narasimhar Overseas

Product: Bliss Tree Ragi Butter Murukku 200g UPC:8906087451754. Packa…
Reason: Undeclared milk
Published: September 25, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 5, 2025Historical recordClass III

Just Right 5000, 1.1% Sodium Fluoride, Candy Apple Flavor, Net Wt. 3.4oz (97g), Rx Only, Manufactured for Elevate Oral Care, LLC in the U.S.A with imported pump, 346 Pike Rd, Suite 5, West Palm Beach, FL 33411, NDC 57511-002-1

by Elevate Oral Care

Reason: LABELING: LABEL MIX-UP.
Published: September 18, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

BARRIER THERAPY SKIN PROTECTANT CREAM (1% colloidal oatmeal), 10 FL OZ/296 ML- tube, Distributed By: Prequel, LOS ANGELES, CA 90069. UPC 8 10129 11007 4

by PREQUEL SKIN

Reason: Microbial contamination of non-sterile Products -
Published: September 18, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 17, 2025Historical recordClass II

American Outdoor Products, Inc.

Product: American Outdoor Products - Astronaut Strawberries, packaged…
Reason: Elevated levels of lead
Published: September 18, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

TIRZEPATIDE 60 mg/3mL (20/mg/mL), Rx Only, 3mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-02

by ProRx LLC

Reason: Lack of Assurance of Sterility
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

TIRZEPATIDE 20 mg/2mL (10/mg/mL), Rx Only, 2mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-01

by ProRx LLC

Reason: Lack of Assurance of Sterility
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Semaglutide / Cyanocobalamin Injection: 2.5/0.5 mg/mL, 2 mL Multiple Dose Vial, Compounded Rx Product, ProRX 267-565-7008, NDC 84139-225-02

by ProRx LLC

Reason: Lack of Assurance of Sterility
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04

by ProRx LLC

Reason: Lack of Assurance of Sterility
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

SEMAGLUTIDE 5mg/2mL (2.5mg/mL), Rx Only 2 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-01

by ProRx LLC

Reason: Lack of Assurance of Sterility
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection vials, Compounded Rx Product, ProRx 267-565-7008, NDC 84139-210-01

by ProRx LLC

Reason: Lack of Assurance of Sterility
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01

by ProRx LLC

Reason: Lack of Assurance of Sterility
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile Single Dose Container, Rx Only, Baxter USA, NDC 0338-0433-04

by Baxter Healthcare Corporation

Reason: Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 12, 2025Historical recordClass I

Unilever North America Supply Chain Company, LLC

Product: Popsicle Jolly Rancher Frozen Confection Pop Net Wt 2.71 FL…
Reason: Undeclared milk
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 29, 2025Historical recordClass II

Cefixime for Oral Suspension USP, 100 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-405-01

by Lupin Pharmaceuticals Inc.

Reason: Subpotent Drug- An out of specification ( OOS ) result observed in assay test during 18-month long term stability study.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

IBU Ibuprofen Tablets, USP, 400 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a) NDC 55111-682-01 - 100 Tablets per bottle, b) NDC 55111-682-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

IBU Ibuprofen Tablets, USP, 600 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-683-01 - 100 Tablets per bottle, b)NDC 5511-683-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

IBU Ibuprofen Tablets, USP, 800 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-684-01 - 100 Tablets per bottle, b)NDC 55111-684-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Indomethacin Extended-Release Capsules, USP, 75 mg, packaged in a) 60-count bottle (NDC 68462-325-60) and b) 90-count bottle (NDC 68462-325-90), Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Plot No. 2 Phase-2, Pharma Zone, SEZ, Pithampur, Dist-Dhar, Madya Pradesh - 454775, India Mfg Llc. No: 25/9/2010, Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: Failed Dissolution Specifications: below specification results
Published: September 4, 2024
Distribution: Nationwide

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Data last updated: October 17, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.